Come Work With Us!

Magenta is a medical device company developing the world’s smallest heart pump, meant to provide minimally-invasive support to the heart during acute episodes of dysfunction. The Elevate™ System is multi-disciplinary, involving mechanical engineering, material science, electrical engineering, software, algorithms and state-of-the-art catheter fabrication techniques.

We are looking for the best people possible who can help us propel the Elevate™ System forward and save more lives.

About the Job

We are looking for a talented mechanical engineer to join our Engineering team and lead multiple processes, facilitating the transition to the manufacturability of a complex product.

Reports to: Engineering Manager

Responsibilities

Design and lead NPI processes such as:

• Collaborate and share data with R&D, production, and quality in integrating and implementing process modification.

• Early engagement with R&D activities and support design updates to be serial-production-worthy documentation.

• Design verification tests- process and fixtures.

• Support production with process-based challenges.

• Design fixtures and jigs to improve manufacturing processes.

• Lead ECO process, support conformity reports.

• Full control on in-scop product’s BOM, DMR and documentation.

Qualifications

• B.S. degree in Mechanical Engineering – must.

• A minimum of 3 years of experience in the medical device industry – must.

• Proficiency in SolidWorks (and PDM) – must.

• Excellent collaboration and communication skills.

• Self-motivated and proactive.

• Fluent in English with excellent writing skills.

 

    Resume*

    About the Job

    We are looking for a Production Engineer who will be part of the leading team of the engineering department.

    Reports to: Engineering & Project Manager

    Responsibilities

    • Responsible for leading and providing cross-functional support configuration management projects such as:

    • Supporting and maintaining the Bill Materials (BOM) management.

    • Building and controlling company’s configuration products, including DMR.

    • Supporting and maintaining ECOs (Engineering Change Orders), including engineering documents, for example: drawings, models, technical data within the PLM system.

    • Technical engineering support for the production and QC department.

    • Work closely with several departments, including R&D, Engineering, Operations, QA, and Product Management.

    Qualifications

    • B.Sc. Engineer in mechanical/ biomedical/ materials science (or other relevant degree).

    • 2-3 years of experience with product BOM (Bill of Material) and change control.

    • Experience in CAD (Solidworks – model & drawings).

    • Knowledge and experience in PDM.

    • Strong organizational skills and attention to detail.

    • Strong analytical skills.

    • Excellent collaboration and communication skills.

    • Self-motivated and proactive.

    • Fluent in English with excellent writing skills.

     

      Resume*

      About the Job

      We are looking for a dynamic and experienced Project Manager who will be part of the leading team of the operations department.

      Reports to: Engineering & Project Manager

      Responsibilities

      As a key member of our team, you will play a pivotal role in coordinating, planning, integrating, and implementing development projects of the company products from early development stages to full transfer for production.

      • Assist with project planning, coordination, and execution: develop detailed project plans, define scope and objectives, and coordinate activities to ensure successful project execution within established timelines.

      • Integration of multidisciplinary systems including mechanics, material, electronics, and software.

      • Collaborate with multidisciplinary teams, including R&D, engineering, QA, and manufacturing.

      • Identification of bottlenecks in existing work processes and definition of appropriate solutions in collaboration with the professional team.

      Qualifications

      • B.Sc. Engineer in mechanical/ biomedical/ materials science (or other relevant degree).

      • 4+ years of experience in a similar role in a medical device company – must.

      • Experience with full product lifecycle, from early development stages to full transfer for production – must.

      • High hands-on technical skills, experience in CAD (Solidworks – Model & Drawings) – must.

      • Excellent communication and interpersonal skills.

      • Ability to lead and motivate cross-functional teams.

      • Excellent writing and verbal skills with strong proficiency in English and Hebrew.

      • Ability to thrive in a fast-paced and dynamic work environment.

       

        Resume*

        About the Job

        We are looking for an experienced Quality Assurance Specialist to join our QA Operations group and support the variety of activities related to QA Operations.

        Reports to: QA Manager

        Responsibilities

        • Lead QA Operations activities with regards to verifications/validations for an FDA reviewed complex, multidisciplinary, active investigational device.

        • Lead and perform the Engineering Change Order (ECO) process from risk analysis through protocol approval.

        • Verification, execution, and analysis of reposts until FDA-ready.

        • Provide guidance to the R&D and Engineering teams on IQ/OQ/PV activities.

        Qualifications

        • B.A. or B.S. degree in a technical discipline, such as Engineering or Science.

        • 5+ years of relevant experience in the medical device industry.

        • Previous experience with medical device verification/validations, ECOs, medical device statistics

        • Working knowledge of medical device international standards.

        • Ability to work independently with minimal work direction and in a cross-functional team environment.

        • Fluent in English with excellent writing skills, effective written and verbal communication skills.

        • Excellent computer skills, including a working knowledge of Microsoft Office applications.

        • Strong time management abilities to ensure timely task completion.

        • Detail-oriented.

          Resume*

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